FUZ, fuzzy planar cell polarity protein, 80199

N. diseases: 75; N. variants: 5
Disease: Congenital cerebral hernia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0014065
Disease: Congenital cerebral hernia
Congenital cerebral hernia 		0.010 GeneticVariation disease BEFREE Although no significant differences in rs202676 genotype or allele frequencies were found between the NTD and control groups, the combined AG+GG genotype group was significantly associated with anencephaly (p = 0.03, OR = 2.11, 95% CI, 1.11-4.01), but not with spina bifida or encephalocele. 22124883 2012